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1دورية أكاديمية
المؤلفون: Winnie Tan, Sylvie van Twest, Andrew Leis, Rohan Bythell-Douglas, Vincent J Murphy, Michael Sharp, Michael W Parker, Wayne Crismani, Andrew J Deans
المصدر: eLife, Vol 9 (2020)
مصطلحات موضوعية: Fanconi anemia, DNA repair, biochemistry, ubiquitin, Medicine, Science, Biology (General), QH301-705.5
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Winnie Tan, Vincent J Murphy, Aude Charron, Sylvie van Twest, Michael Sharp, Angelos Constantinou, Michael W Parker, Wayne Crismani, Rohan Bythell-Douglas, Andrew J Deans
المصدر: PLoS ONE, Vol 15, Iss 2, p e0229000 (2020)
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1932-6203
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3دورية أكاديمية
المؤلفون: Sile F. Yang, Christopher B. Nelson, Jadon K. Wells, Madushan Fernando, Robert Lu, Joshua A. M. Allen, Lisa Malloy, Noa Lamm, Vincent J. Murphy, Joel P. Mackay, Andrew J. Deans, Anthony J. Cesare, Alexander P. Sobinoff, Hilda A. Pickett
المصدر: Nature Communications, Vol 15, Iss 1, Pp 1-15 (2024)
مصطلحات موضوعية: Science
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2041-1723
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المؤلفون: Charlotte Hodson, Sylvie van Twest, Malgorzata Dylewska, Julienne J. O’Rourke, Winnie Tan, Vincent J. Murphy, Mannu Walia, Lara Abbouche, Jadwiga Nieminuszczy, Elyse Dunn, Rohan Bythell-Douglas, Jörg Heierhorst, Wojciech Niedzwiedz, Andrew J. Deans
المصدر: Cell reports. 41(10)
مصطلحات موضوعية: General Biochemistry, Genetics and Molecular Biology
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المؤلفون: Andrew Leis, Rohan Bythell-Douglas, Michael W. Parker, Sylvie van Twest, Wayne Crismani, Andrew J. Deans, Vincent J. Murphy, Winnie Tan, Michael F. Sharp
مصطلحات موضوعية: Core (optical fiber), chemistry.chemical_compound, Chemistry, Fanconi anemia, FANCD2, medicine, Monoubiquitination, medicine.disease, DNA, Cell biology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::69090c66409361c7137c9662e9f9ad25
https://doi.org/10.7554/elife.54128.sa2 -
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المؤلفون: Sylvie van Twest, Winnie Tan, Vincent J. Murphy, Andrew J. Deans
المصدر: Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology, Vol 8 (2020)مصطلحات موضوعية: 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, DNA repair, DNA damage, ubiquitination, Deubiquitinating enzyme, Cell and Developmental Biology, 03 medical and health sciences, 0302 clinical medicine, Ubiquitin, hemic and lymphatic diseases, FANCD2, FANCI, Monoubiquitination, lcsh:QH301-705.5, deubiquitination, biology, phosphorylation, Chemistry, nutritional and metabolic diseases, Cell Biology, DNA Repair Pathway, Brief Research Report, 3. Good health, Cell biology, 030104 developmental biology, lcsh:Biology (General), 030220 oncology & carcinogenesis, biology.protein, Developmental Biology, Deubiquitination
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb41eb91044fe0b5f70769b8a5d20f6f
https://doi.org/10.3389/fcell.2020.00002 -
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المؤلفون: Fenil Shah, Andrew J. Deans, Aaron J. Borg, Ludovic Renault, Alessandro Costa, Paolo Swuec, Sylvie van Twest, Vincent J. Murphy, Ambrosius P. Snijders
المصدر: Cell Reports
Cell Reports, Vol 18, Iss 3, Pp 611-623 (2017)مصطلحات موضوعية: 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, DNA repair, Protein subunit, cryo-electron microscopy, interstrand crosslink, ubiquitin ligase, General Biochemistry, Genetics and Molecular Biology, Article, Mass Spectrometry, Substrate Specificity, 03 medical and health sciences, Protein structure, Fanconi anemia, hemic and lymphatic diseases, FANCD2, medicine, Humans, FANCL, Amino Acid Sequence, lcsh:QH301-705.5, Chromatography, High Pressure Liquid, biology, Chemistry, Fanconi Anemia Complementation Group D2 Protein, Ubiquitination, nutritional and metabolic diseases, medicine.disease, mono-ubiquitination, Fanconi Anemia Complementation Group Proteins, 3. Good health, FANCB, Ubiquitin ligase, Protein Structure, Tertiary, DNA-Binding Proteins, Microscopy, Electron, 030104 developmental biology, lcsh:Biology (General), Biochemistry, Biophysics, biology.protein, Protein Multimerization, Dimerization
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المؤلفون: Winnie Tan, Rasim Ozgur Rosti, Moonjung Jung, Arleen D. Auerbach, Danielle C. Kimble, Ramanagouda Ramanagoudr-Bhojappa, Settara C. Chandrasekharappa, Francis P. Lach, Sylvie van Twest, Carlo Doufour, Parinda A. Mehta, Agata Smogorzewska, Frank X. Donovan, Caroline S. Jiang, Vincent J. Murphy, Andrew J. Deans, Roger D. Vaughan, Filomena Pierri
مصطلحات موضوعية: Genetics, 0303 health sciences, 030305 genetics & heredity, Bone marrow failure, Biology, medicine.disease, 3. Good health, FANCB, Complementation, 03 medical and health sciences, Fanconi anemia, hemic and lymphatic diseases, FANCD2, medicine, Missense mutation, Monoubiquitination, Gene, 030304 developmental biology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65144693d5918a24dcddb29a7095970c
https://doi.org/10.1101/772574 -
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المؤلفون: Frank X. Donovan, Winnie Tan, Sylvie van Twest, Carlo Dufour, Caroline S. Jiang, Andrew J. Deans, Danielle C. Kimble, Settara C. Chandrasekharappa, Moonjung Jung, Roger D. Vaughan, Agata Smogorzewska, Parinda A. Mehta, Vincent J. Murphy, Filomena Pierri, Francis P. Lach, Rasim Ozgur Rosti, Ramanagouda Ramanagoudr-Bhojappa, Arleen D. Auerbach
المصدر: Blood
مصطلحات موضوعية: 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, RNA Stability, Immunology, 030105 genetics & heredity, Biology, medicine.disease_cause, Biochemistry, Models, Biological, Severity of Illness Index, 03 medical and health sciences, Red Cells, Iron, and Erythropoiesis, Fanconi anemia, hemic and lymphatic diseases, Cell Line, Tumor, FANCD2, medicine, Monoubiquitination, Missense mutation, Humans, Genetic Predisposition to Disease, Allele, Alleles, Genetic Association Studies, Genetics, Mutation, Bone marrow failure, Ubiquitination, nutritional and metabolic diseases, Genetic Variation, Cell Biology, Hematology, Fibroblasts, medicine.disease, Fanconi Anemia Complementation Group Proteins, FANCB, Alternative Splicing, 030104 developmental biology, Fanconi Anemia, Phenotype, Genetic Loci
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baffc3cd63c0f967d11a3ceeb903240b
https://pubmed.ncbi.nlm.nih.gov/32353126 -
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المؤلفون: Joerg Heierhorst, Rui Liu, Monique Smeets, Charlotte Hodson, Carl R. Walkley, Wilson Castillo-Tandazo, Vincent J. Murphy, Andrew J. Deans
المصدر: PLoS Genetics, Vol 15, Iss 7, p e1008266 (2019)
PLoS Geneticsمصطلحات موضوعية: Cancer Research, B Cells, RecQ helicase, T-Lymphocytes, QH426-470, medicine.disease_cause, Biochemistry, Mice, White Blood Cells, 0302 clinical medicine, Adenosine Triphosphate, Animal Cells, Medicine and Health Sciences, ATP-dependent helicase activity, Gene Knock-In Techniques, Rothmund–Thomson syndrome, Genetics (clinical), 0303 health sciences, Mutation, B-Lymphocytes, biology, RecQ Helicases, T Cells, Rothmund-Thomson Syndrome, Phenotype, Null allele, Cell biology, Enzymes, Nucleic acids, Helicases, Cellular Types, Research Article, Immune Cells, Immunology, Embryonic Development, 03 medical and health sciences, Protein Domains, DNA-binding proteins, medicine, Genetics, Animals, Humans, Point Mutation, Antibody-Producing Cells, Molecular Biology, Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, Binding Sites, Blood Cells, Point mutation, Body Weight, Helicase, Biology and Life Sciences, Proteins, Cell Biology, DNA, medicine.disease, Hematopoiesis, Disease Models, Animal, biology.protein, Enzymology, DNA damage, 030217 neurology & neurosurgery